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Human Heredity|February 16, 2022
Genetic Analyses of Enamel Hypoplasia in Multiethnic CohortsRasha N Alotaibi, Brian J Howe, Lina M Moreno Uribe, et al.
Dentistry Journal|July 25, 2022
Tooth Agenesis Patterns in Orofacial Clefting Using Tooth Agenesis Code: A Meta-AnalysisBrian J Howe, Chandler Pendleton, Miyuraj Harishchandra Hikkaduwa Withanage, et al.
Plos Genetics|August 26, 2016
Genome-Wide Association Study Reveals Multiple Loci Influencing Normal Human Facial MorphologyJohn R Shaffer, Ekaterina Orlova, Myoung Keun Lee, et al.
Genetic Epidemiology|November 11, 2017
Identification of 16q21 as a modifier of nonsyndromic orofacial cleft phenotypesJenna C Carlson, Jennifer Standley, Aline Petrin, et al.
Medrxiv : the Preprint Server for Health Sciences|March 27, 2026
Trio-based GWAS reveals novel loci associated with different forms of isolated cleft lipNoah Herrick, Zeynep Erdogan-Yildirim, Myoung Keun Lee, et al.
Human Molecular Genetics|September 26, 2009
FOXE1 association with both isolated cleft lip with or without cleft palate, and isolated cleft palateLina M Moreno, Maria Adela Mansilla, Steve A Bullard, et al.
American Journal of Human Genetics|June 24, 2020
Genome-wide Enrichment of De Novo Coding Mutations in Orofacial Cleft TriosMadison R Bishop, Kimberly K Diaz Perez, Miranda Sun, et al.
American Journal of Human Genetics|December 5, 2017
Multiethnic GWAS Reveals Polygenic Architecture of Earlobe AttachmentJohn R Shaffer, Jinxi Li, Myoung Keun Lee, et al.
Human Mutation|June 20, 2019
Mutations in GDF11 and the extracellular antagonist, Follistatin, as a likely cause of Mendelian forms of orofacial clefting in humansTimothy C Cox, Andrew C Lidral, Jason C McCoy, et al.
Medrxiv : the Preprint Server for Health Sciences|June 4, 2026
Comprehensive analysis of <i>de novo</i> variants across 2,497 orofacial cleft trios reveals novel genetic drivers of diseaseNehir E Kurtas, Alba Sanchis-Juan, Eren Shin, et al.
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